Canonical Allele Identifier: CA249263523
Gene: HTR2A HGNC NCBI

Linked Data

dbSNP Id: rs952811665
gnomAD v2: 13-47471453-A-G
gnomAD v3: 13-46897318-A-G
gnomAD v4: 13-46897318-A-G
MyVariant Identifiers: chr13:g.47471453A>G (hg19) chr13:g.46897318A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.46897318A>G , CM000675.2:g.46897318A>G GRCh38
NC_000013.10:g.47471453A>G , CM000675.1:g.47471453A>G GRCh37
NC_000013.9:g.46369454A>G NCBI36
NG_013011.1:g.4717T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001378924.1:c.-329+634T>C NP_001365853.1:n.-329+634T>C
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